Canonical Allele Identifier: CA2582590992

Gene: STK11

Linked Data

• gnomAD v4: 19-1206682-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1206685del , CM000681.2:g.1206685del	GRCh38
NC_000019.9:g.1206684del , CM000681.1:g.1206684del	GRCh37
NC_000019.8:g.1157684del	NCBI36
NG_007460.2:g.22279del , LRG_319:g.22279del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.-229del	ENSP00000490268.2:n.-229del
ENST00000585748.3:c.-82-11732del	ENSP00000477641.2:n.-82-11732del
ENST00000326873.12:c.-229del MANE Select	ENSP00000324856.6:n.-229del
ENST00000652231.1:c.-229del	ENSP00000498804.1:n.-229del
ENST00000326873.11:c.-229del	ENSP00000324856.6:n.-229del
ENST00000585748.2:c.-82-11732del	ENSP00000477641.1:n.-82-11732del
ENST00000586243.5:c.-229del	ENSP00000467240.2:n.-229del
NM_000455.4:c.-229del , LRG_319t1:c.-229del	NP_000446.1:n.-229del
XM_005259617.1:c.-229del	XP_005259674.1:n.-229del
XM_005259618.3:c.-229del	XP_005259675.1:n.-229del
XM_011528209.1:c.-582del	XP_011526511.1:n.-582del
XR_936204.1:n.397del
XM_005259617.3:c.-229del	XP_005259674.1:n.-229del
XM_011528209.2:c.-582del	XP_011526511.1:n.-582del
XR_001753738.2:n.397del
XR_001753739.1:n.397del
XR_001753740.2:n.397del
NM_000455.5:c.-229del MANE Select	NP_000446.1:n.-229del